A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5656



Internal ID15543777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:41264025..41300756hg38UCSC Ensembl
Outerchr17:39420277..39457008hg19UCSC Ensembl
Outerchr17:36673803..36710534hg18UCSC Ensembl
Outerchr17:36673803..36710534hg17UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3836732
hg1936732
hg1836732
hg1736732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2050
Supporting Variants
SamplesNA19129
Known GenesKRTAP9-6, KRTAP9-7
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv5656
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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